# FDA Inspection 1097565 - Kimberly-Clark Corporation Cold Spring - July 25, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/kimberly-clark-corporation-cold-spring/27ad9673-684e-4308-830f-5633766ccf71
Source feed: FDA_Inspections

> FDA Inspection 1097565 for Kimberly-Clark Corporation Cold Spring on July 25, 2019. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1097565
- Company Name: Kimberly-Clark Corporation Cold Spring
- Inspection Date: 2019-07-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1097565 - 2019-07-25](https://www.globalkeysolutions.net/records/fda_inspections/kimberly-clark-corporation-cold-spring/5a556498-0261-41e4-96f9-785205c11fa5)
- [FDA Inspection 720291 - 2011-03-02](https://www.globalkeysolutions.net/records/fda_inspections/kimberly-clark-corporation-cold-spring/64e043fc-d5fe-4d95-9fa0-d7dd0639ac2c)

Company: https://www.globalkeysolutions.net/companies/kimberly-clark-corporation-cold-spring/3a19488b-8ad1-4fae-8f27-f0e1da1f624e

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7